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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Light, Ultraviolet, Dermatological
510(k) Number K844870
Device Name SUNTAN CONNECTIONS BAHAMA SUN-BOOTH
Applicant
Suntan Connection
2416 San Carlos Ave.
Castro Valley,  CA  94546
Applicant Contact JEFFREY P COLLINS
Correspondent
Suntan Connection
2416 San Carlos Ave.
Castro Valley,  CA  94546
Correspondent Contact JEFFREY P COLLINS
Regulation Number878.4630
Classification Product Code
FTC  
Date Received12/03/1984
Decision Date 01/09/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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